ClinVar Miner

List of variants in gene USH2A reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 152
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HGVS dbSNP
NM_206933.3(USH2A):c.10062G>C (p.Val3354=) rs200172376
NM_206933.3(USH2A):c.10232= (p.Glu3411=) rs10864198
NM_206933.3(USH2A):c.10232A>C (p.Glu3411Ala) rs10864198
NM_206933.3(USH2A):c.10510C>G (p.Pro3504Ala) rs200372118
NM_206933.3(USH2A):c.10552G>A (p.Val3518Ile) rs75397806
NM_206933.3(USH2A):c.10836C>A (p.Val3612=) rs61276761
NM_206933.3(USH2A):c.10851C>T (p.Asn3617=) rs12073994
NM_206933.3(USH2A):c.10858A>G (p.Ile3620Val) rs145207584
NM_206933.3(USH2A):c.11048-15C>T rs74141403
NM_206933.3(USH2A):c.11191G>C (p.Glu3731Gln) rs150264392
NM_206933.3(USH2A):c.11389+9A>T rs12095085
NM_206933.3(USH2A):c.11404G>A (p.Glu3802Lys) rs147900972
NM_206933.3(USH2A):c.11504C>T (p.Thr3835Ile) rs11120616
NM_206933.3(USH2A):c.11549-16dup rs34565443
NM_206933.3(USH2A):c.11549-5del rs34565443
NM_206933.3(USH2A):c.11602A>G (p.Met3868Val) rs35309576
NM_206933.3(USH2A):c.11677C>A (p.Pro3893Thr) rs41303285
NM_206933.3(USH2A):c.11736G>A (p.Glu3912=) rs56053654
NM_206933.3(USH2A):c.11794C>T (p.Leu3932=) rs111033505
NM_206933.3(USH2A):c.11907A>T (p.Pro3969=) rs61635304
NM_206933.3(USH2A):c.11928G>A (p.Thr3976=) rs55961436
NM_206933.3(USH2A):c.11946G>A (p.Leu3982=) rs2820718
NM_206933.3(USH2A):c.12046G>A (p.Val4016Met) rs138803855
NM_206933.3(USH2A):c.12093C>T (p.Tyr4031=) rs55921307
NM_206933.3(USH2A):c.12445T>C (p.Trp4149Arg) rs115884084
NM_206933.3(USH2A):c.12608A>G (p.Gln4203Arg) rs148556640
NM_206933.3(USH2A):c.12612= (p.Thr4204=) rs2797235
NM_206933.3(USH2A):c.12612G>A (p.Thr4204=) rs2797235
NM_206933.3(USH2A):c.12666A>G (p.Thr4222=) rs2797234
NM_206933.3(USH2A):c.12743A>G (p.His4248Arg) rs145830318
NM_206933.3(USH2A):c.12817T>C (p.Tyr4273His) rs79654794
NM_206933.3(USH2A):c.13134G>T (p.Pro4378=) rs148975669
NM_206933.3(USH2A):c.13191G>A (p.Glu4397=) rs2009923
NM_206933.3(USH2A):c.13297G>T (p.Val4433Leu) rs111033381
NM_206933.3(USH2A):c.13404A>G (p.Arg4468=) rs146994147
NM_206933.3(USH2A):c.13440G>A (p.Arg4480=) rs111033378
NM_206933.3(USH2A):c.13478G>A (p.Arg4493His) rs138879998
NM_206933.3(USH2A):c.13709G>A (p.Arg4570His) rs730254
NM_206933.3(USH2A):c.13763C>A (p.Ser4588Tyr) rs78253373
NM_206933.3(USH2A):c.13857A>G (p.Ser4619=) rs373694614
NM_206933.3(USH2A):c.13984C>G (p.Gln4662Glu) rs41302237
NM_206933.3(USH2A):c.14074G>A (p.Gly4692Arg) rs45549044
NM_206933.3(USH2A):c.1419C>T (p.Thr473=) rs1805050
NM_206933.3(USH2A):c.14226G>A (p.Thr4742=) rs78576418
NM_206933.3(USH2A):c.14315C>T (p.Ser4772Phe) rs149222801
NM_206933.3(USH2A):c.14333C>A (p.Ala4778Asp) rs113447586
NM_206933.3(USH2A):c.1434G>C (p.Glu478Asp) rs35730265
NM_206933.3(USH2A):c.14454G>A (p.Pro4818=) rs137902779
NM_206933.3(USH2A):c.14481C>T (p.Ala4827=) rs41304083
NM_206933.3(USH2A):c.14513G>A (p.Gly4838Glu) rs41315587
NM_206933.3(USH2A):c.14517G>A (p.Thr4839=) rs397517991
NM_206933.3(USH2A):c.14543G>A (p.Arg4848Gln) rs77211159
NM_206933.3(USH2A):c.14662A>T (p.Thr4888Ser) rs200993435
NM_206933.3(USH2A):c.14960C>T (p.Ala4987Val) rs111033498
NM_206933.3(USH2A):c.15076A>G (p.Lys5026Glu) rs41308435
NM_206933.3(USH2A):c.15091C>T (p.Arg5031Trp) rs56038610
NM_206933.3(USH2A):c.15297+3A>G rs57754754
NM_206933.3(USH2A):c.15377T>C (p.Ile5126Thr) rs111033266
NM_206933.3(USH2A):c.15427C>T (p.Arg5143Cys) rs145771342
NM_206933.3(USH2A):c.15428G>A (p.Arg5143His) rs111033435
NM_206933.3(USH2A):c.15433G>A (p.Val5145Ile) rs111033269
NM_206933.3(USH2A):c.15522T>C (p.Tyr5174=) rs77792891
NM_206933.3(USH2A):c.15562A>G (p.Ser5188Gly) rs58257972
NM_206933.3(USH2A):c.1608C>T (p.Cys536=) rs187380128
NM_206933.3(USH2A):c.1731C>T (p.Cys577=) rs41313732
NM_206933.3(USH2A):c.1840+19C>G rs886038764
NM_206933.3(USH2A):c.1931A>T (p.Asp644Val) rs1805048
NM_206933.3(USH2A):c.2052A>G (p.Gln684=) rs111033248
NM_206933.3(USH2A):c.2094C>T (p.Thr698=) rs141489104
NM_206933.3(USH2A):c.2109T>C (p.Asp703=) rs45555435
NM_206933.3(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.3(USH2A):c.2510G>A (p.Arg837Gln) rs148594393
NM_206933.3(USH2A):c.2522C>A (p.Ser841Tyr) rs111033282
NM_206933.3(USH2A):c.2546G>A (p.Cys849Tyr) rs111033481
NM_206933.3(USH2A):c.2633G>A (p.Arg878His) rs200124505
NM_206933.3(USH2A):c.3364T>G (p.Ser1122Ala) rs148135241
NM_206933.3(USH2A):c.3395G>A (p.Gly1132Asp) rs34596189
NM_206933.3(USH2A):c.3532C>G (p.Pro1178Ala) rs372081834
NM_206933.3(USH2A):c.3621C>T (p.Ile1207=) rs146462407
NM_206933.3(USH2A):c.3648C>T (p.Tyr1216=) rs147947402
NM_206933.3(USH2A):c.373G>A (p.Ala125Thr) rs10779261
NM_206933.3(USH2A):c.3812-8T>G rs646094
NM_206933.3(USH2A):c.3945T>C (p.Asn1315=) rs41303257
NM_206933.3(USH2A):c.4252-36CTTT[5] rs372388546
NM_206933.3(USH2A):c.4371G>A (p.Ser1457=) rs56013136
NM_206933.3(USH2A):c.4440C>T (p.Ser1480=) rs111632670
NM_206933.3(USH2A):c.4457= (p.Lys1486=) rs1805049
NM_206933.3(USH2A):c.4457A>G (p.Lys1486Arg) rs1805049
NM_206933.3(USH2A):c.4543A>G (p.Thr1515Ala) rs141671082
NM_206933.3(USH2A):c.4560C>T (p.Ile1520=) rs148000219
NM_206933.3(USH2A):c.4586A>T (p.Lys1529Ile) rs41303255
NM_206933.3(USH2A):c.4714C>T (p.Leu1572Phe) rs111033333
NM_206933.3(USH2A):c.4758+3A>G rs117798425
NM_206933.3(USH2A):c.478G>A (p.Gly160Ser) rs111033479
NM_206933.3(USH2A):c.486-13G>A rs116367260
NM_206933.3(USH2A):c.504A>G (p.Thr168=) rs4253963
NM_206933.3(USH2A):c.573A>G (p.Val191=) rs73102592
NM_206933.3(USH2A):c.5932C>T (p.Pro1978Ser) rs75698489
NM_206933.3(USH2A):c.5975A>G (p.Tyr1992Cys) rs41303287
NM_206933.3(USH2A):c.5993G>A (p.Arg1998His) rs143624066
NM_206933.3(USH2A):c.6001C>T (p.Arg2001Cys) rs141539554
NM_206933.3(USH2A):c.6041A>C (p.Asn2014Thr) rs147883884
NM_206933.3(USH2A):c.6077A>G (p.Lys2026Arg) rs115039883
NM_206933.3(USH2A):c.6186A>C (p.Pro2062=) rs200247886
NM_206933.3(USH2A):c.6236A>C (p.Lys2079Thr) rs147039836
NM_206933.3(USH2A):c.6240G>T (p.Lys2080Asn) rs114402911
NM_206933.3(USH2A):c.6257C>A (p.Thr2086Asn) rs149202379
NM_206933.3(USH2A):c.6270A>G (p.Leu2090=) rs56245532
NM_206933.3(USH2A):c.6317= (p.Thr2106=) rs6657250
NM_206933.3(USH2A):c.6317C>T (p.Thr2106Ile) rs6657250
NM_206933.3(USH2A):c.6369C>T (p.Cys2123=) rs111033472
NM_206933.3(USH2A):c.6506T>C (p.Ile2169Thr) rs10864219
NM_206933.3(USH2A):c.6510T>G (p.Ser2170Arg) rs373604102
NM_206933.3(USH2A):c.6587G>C (p.Ser2196Thr) rs79444516
NM_206933.3(USH2A):c.6628C>G (p.Pro2210Ala) rs192115090
NM_206933.3(USH2A):c.6683T>A (p.Val2228Glu) rs117461552
NM_206933.3(USH2A):c.6713A>C (p.Glu2238Ala) rs41277212
NM_206933.3(USH2A):c.6875G>A (p.Arg2292His) rs41277210
NM_206933.3(USH2A):c.688G>A (p.Val230Met) rs45500891
NM_206933.3(USH2A):c.6957+19A>G rs6689120
NM_206933.3(USH2A):c.7068T>G (p.Asn2356Lys) rs200038092
NM_206933.3(USH2A):c.7121-14del rs536181325
NM_206933.3(USH2A):c.7130A>G (p.Asn2377Ser) rs111033394
NM_206933.3(USH2A):c.7160T>C (p.Met2387Thr) rs115015305
NM_206933.3(USH2A):c.7506G>A (p.Pro2502=) rs12404427
NM_206933.3(USH2A):c.7584C>T (p.Thr2528=) rs78250390
NM_206933.3(USH2A):c.7685T>C (p.Val2562Ala) rs56385601
NM_206933.3(USH2A):c.785-16_785-15del rs150209313
NM_206933.3(USH2A):c.78T>C (p.Ala26=) rs59139861
NM_206933.3(USH2A):c.8315C>T (p.Thr2772Ile) rs150807452
NM_206933.3(USH2A):c.8319C>T (p.Ser2773=) rs56829872
NM_206933.3(USH2A):c.8458G>A (p.Val2820Ile) rs59174500
NM_206933.3(USH2A):c.848+5G>C rs74329863
NM_206933.3(USH2A):c.8558+40C>A rs55713064
NM_206933.3(USH2A):c.8624G>A (p.Arg2875Gln) rs12118814
NM_206933.3(USH2A):c.8656C>T (p.Leu2886Phe) rs41277200
NM_206933.3(USH2A):c.8681+18A>G rs41277198
NM_206933.3(USH2A):c.879T>G (p.Leu293=) rs3767698
NM_206933.3(USH2A):c.8937A>G (p.Val2979=) rs139100097
NM_206933.3(USH2A):c.9110G>A (p.Arg3037His) rs533700989
NM_206933.3(USH2A):c.9213G>A (p.Ser3071=) rs111033397
NM_206933.3(USH2A):c.9259-14A>C rs561590242
NM_206933.3(USH2A):c.9262G>A (p.Glu3088Lys) rs56056328
NM_206933.3(USH2A):c.9296A>G (p.Asn3099Ser) rs41277194
NM_206933.3(USH2A):c.9340C>T (p.Pro3114Ser) rs201071654
NM_206933.3(USH2A):c.9343A>G (p.Thr3115Ala) rs56032526
NM_206933.3(USH2A):c.9430G>A (p.Asp3144Asn) rs11120645
NM_206933.3(USH2A):c.9459C>T (p.Cys3153=) rs73090721
NM_206933.3(USH2A):c.9595A>G (p.Asn3199Asp) rs4129843
NM_206933.3(USH2A):c.9723C>T (p.Tyr3241=) rs6660707
NM_206933.3(USH2A):c.9915G>C (p.Glu3305Asp) rs145278250
NM_206933.3(USH2A):c.9959-11T>G rs116150014

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